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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096805copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318 SNORA94, LIMD1-AS1, 120 more genes
    nsv6713770copy number variation1nstd229human GRCh38 chr3: 48,549,807-48,561,811 , GRCh37.p13 chr3: 48,587,240-48,599,244 PFKFB4, MIR6823, 1 more genes
    nsv6708120copy number variation1nstd229human GRCh38 chr3: 48,552,177-48,594,105 , GRCh37.p13 chr3: 48,589,610-48,631,538 MIR711, UCN2, 2 more genes
    nsv6700836copy number variation1nstd229human GRCh38 chr3: 48,056,801-51,204,000 , GRCh37.p13 chr3: 48,098,291-51,241,431 APEH, SLC26A6, 129 more genes
    nsv6372055copy number variation1nstd223human GRCh38 chr3: 48,386,801-49,230,000 , GRCh37.p13 chr3: 48,428,291-49,267,433 NCKIPSD, UCN2, 44 more genes
    nsv6365306copy number variation1nstd223human GRCh38 chr3: 48,429,601-48,926,800 , GRCh37.p13 chr3: 48,471,010-48,964,233 PRKAR2A-AS1, SNORA94, 25 more genes
    nsv6315166copy number variation1nstd102humanPathogenic GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376 TMEM89, TGM4, 129 more genes
    nsv6164129copy number variation1nstd214human GRCh38 chr3: 48,561,633-48,561,723 , GRCh37.p13 chr3: 48,599,066-48,599,156 UCN2, PFKFB4
    nsv6155021copy number variation1nstd214human GRCh38 chr3: 48,561,698-48,561,788 , GRCh37.p13 chr3: 48,599,131-48,599,221 UCN2, PFKFB4
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv6066537insertion1nstd212human GRCh38 chr3: 48,561,734-48,561,734 , GRCh37.p13 chr3: 48,599,167-48,599,167 PFKFB4, UCN2
    nsv5993411copy number variation1nstd212human GRCh38 chr3: 48,561,650-48,561,742 , GRCh37.p13 chr3: 48,599,083-48,599,175 PFKFB4, UCN2
    nsv5905002copy number variation1nstd209human GRCh38 chr3: 48,561,633-48,561,723 , GRCh37.p13 chr3: 48,599,066-48,599,156 PFKFB4, UCN2
    nsv5673729copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,507,870-50,340,407 , GRCh38.p12 chr3: 48,466,471-50,302,976 SEMA3B-AS1, GNAT1, 87 more genes
    nsv5580428copy number variation1nstd207human GRCh38 chr3: 48,561,633-48,561,723 , GRCh37.p13 chr3: 48,599,066-48,599,156 UCN2, PFKFB4
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
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